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Structure of 1368352-40-2
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5-Bromo-4-ethylpyridin-2-amine features a bromine substituent at the 5-position and an ethyl group at the 4-position on a pyridine ring bearing a primary amine at the 2-position. This electron-deficient heterocycle integrates readily into cross-coupling reactions, enabling efficient access to functionalized pyridine scaffolds under standard conditions.
5-Bromo-4-ethylpyridin-2-amine serves as a versatile building block in medicinal chemistry and catalytic synthesis. Its pyridine core enables transition-metal-catalyzed cross-coupling reactions, while the bromo and amine groups offer orthogonal reactivity for sequential functionalization. The ethyl substituent enhances solubility and modulates electronic properties, contributing to favorable handling and purification. This compound functions effectively in Suzuki-Miyaura, Buchwald-Hartwig, and related transformations, facilitating access to complex heterocyclic scaffolds common in pharmaceutical development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: